119 Clinical Data And Biostatistics jobs in San Francisco.

Redwood City

• Skills: clinical regulatory affairs, regulatory submissions, IND filings, BLA filings, regulatory strategy, compliance, pharmaceutical industry, project management, communication skills, cell therapies
• Experience: 12-15+ years of clinical regulatory affairs experience
• Type: Full-time
• Salary: $275,000 - $305,000 per year

Palo Alto

• Skills: Endocrinology, Clinical Development Plan, Clinical trials, Medical Monitor, Regulatory strategy, Clinical data analysis, Cross-functional collaboration, Clinical trial design, Scientific inquiry, Patient-focused therapies
• Experience: At least 5 years of industry experience, at least 3 years of experience with clinical trial design and execution
• Type: Full-time
• Salary: $265-285K/year

Oakland

• Skills: clinical content strategy, oncology pharmacy, data-driven planning, evidence-based content, clinical data tools, Python, SQL, compliance, cross-functional collaboration, patient education resources
• Experience: 4+ years of experience in a patient-facing oncology role
• Type: Full-time
• Salary: Competitive Salary: aligned with market standards

South San Francisco

• Skills: drug safety, safety monitoring, signal detection, regulatory standards, Risk Management Plans, Risk Evaluation, Mitigation Strategies, regulatory documents, collaboration, process improvements
• Type: Full-time

Fremont

• Skills: Brain-Computer Interface, BCI, user needs, data collection, communication skills, clinical studies, experiment methodology, data analysis, neural decoding, user experience
• Experience: Experience working with users for a product or service, Experience in data collection and analysis (in Python)
• Type: Full-time
• Salary: $89,000 — $148,000 USD

San Francisco

• Skills: clinical trial management, project timeline adherence, quality delivery, clinical research, monitoring, regulatory documentation, data cleaning, collaborative environment, communication skills, clinical trial activities
• Experience: 5-7 years of clinical research experience with significant clinical monitoring experience.
• Type: Full-time

San Francisco

• Skills: clinical data management, real-world data, data abstraction, EHR, quality control, regulatory requirements, data analysis, project management, healthcare IT systems, clinical research applications
• Experience: 3+ years working with ophthalmology or urology clinical data
• Type: Full-time
• Salary: $145,000—$180,000 USD

Menlo Park

• Skills: healthcare data, Clinical Data, deep analysis, LLMs, pre-visit clinical summaries, engagement reporting, anomaly detection, data warehouse, medical data errors, analytics
• Experience: At least 5 years of general engineering experience
• Type: Full-time

Redwood City

• Skills: Pharmacokinetics, Biomarker analyses, statistical expert, clinical program teams, clinical documents, clinical protocol, statistical analysis plan, PK modeling, biomarker analysis, CDISC standards
• Experience: 12 years of relevant experience with MS/MA degree, or 8 years with PhD in related discipline
• Type: Full-time
• Salary: $240,000 - $255,000 per year

South San Francisco

• Skills: clinical pharmacology, drug development, data analysis, pharmacokinetics, regulatory submissions, clinical trials, translational science, quantitative pharmacology, vendor management, cross-functional collaboration
• Experience: PhD in Pharmacology and/or PharmD with at least 3+ years of industry experience in clinical pharmacology or pharmacometrics
• Type: Full-time
• Salary: $203,000 to $248,000

Redwood City

• Skills: data management, clinical studies, database activities, protocol review, data integrity, data cleaning, oncology, Medidata RAVE, regulatory guidelines, communication skills
• Experience: Minimum of 7 years of clinical data management experience in the pharmaceutical, biotechnology industry or in a CRO.
• Type: Full-time
• Salary: $180,000 - $195,000 per year

Palo Alto

• Skills: auditing, clinical documentation improvement, ICD-10 coding, DRG coding, analysis, medical records, claims auditing, billing guidelines, payment systems, health information
• Experience: Minimum of 10 years in claims auditing and 5 years with ICD-9/10CM
• Type: Hybrid
• Salary: $79,268 to $150,192

Alameda

• Skills: medical coding, clinical trials, coding strategy, vendor partnerships, ICH-GCP guidelines, clinical data management, project management, MedDRA, WHODrug, coding expertise
• Experience: 11+ years of related experience
• Type: Full-time
• Salary: $141,000 - $199,500

San Rafael

• Skills: Medical Writing, Clinical Studies, Submissions, Document Preparation, Protocols, Informed Consent Forms, Safety Reports, Regulatory Submissions, Documentation Management, Biotechnology
• Experience: At least 5 years experience required
• Type: Contract
• Salary: null to null per hour

Palo Alto

• Skills: Hematology, Oncology, clinical development, medical monitoring, regulatory interactions, clinical trial data, safety findings, strategic input, clinical protocols, external relationships
• Experience: 3+ years academic and/or pharmaceutical industry experience
• Type: Full-time
• Salary: $240,000.00 - $360,000.00

San Rafael

• Skills: Medical Writing, Clinical Development, Regulatory Submissions, Documentation, Resource Planning, Vendor Management, Clinical Studies, Team Leadership, Budget Management, Cross-Functional Collaboration
• Experience: At least 10 years of experience as a medical writer in the pharmaceutical industry.
• Type: Hybrid

Menlo Park

• Skills: clinical data management, data integrity, clinical programs, strategic leadership, operational expertise, high-quality data solutions, decision-making, regulatory submissions

South San Francisco

• Skills: biostatistics, clinical development, study design, regulatory submissions, statistical analysis, SAS, R programming, clinical study protocols, vendor management, leadership
• Experience: 7+ years of experience working in early- and late-stage clinical development in the pharma/biotech industry.
• Salary: $225,000 to 275,000

Menlo Park

• Skills: data management, clinical trials, CDISC compliance, EDC systems, SOPs, data quality, project management, pharmacovigilance, biomedical data, data visualization
• Experience: 12+ years experience in clinical trial industry (med device, pharma or biotech), 10+ years experience in data management in clinical trial industry.

Oakland

• Skills: data management, clinical data management, project management, negotiations, quality management, financial tracking, process improvements, Good Clinical Practices, regulatory guidelines, compliance
• Experience: 5 years direct Data Management experience, including 3 or more years as a CDM project lead.
• Type: Full time
• Salary: $82,300.00 - $173,900.00

Sunnyvale

• Skills: clinical studies, evidence generation, clinical protocols, project management, regulatory compliance, biostatistics, clinical research, data analysis, stakeholder engagement, medical device trials
• Experience: Minimum Advanced degree in a scientific/bioengineering field (M.S., Ph.D. or M.D.) with a minimum of 5 years of experience in clinical research, or Bachelor’s degree in a scientific/bioengineering field with a minimum of 8 years of experience in clinical research is preferred, or a minimum of 10 years of experience in clinical research with relevant training.
• Type: Clinical & Medical Affairs

Santa Clara

• Skills: clinical support, interventional procedures, medical devices, clinical studies, training materials, data collection, hospital systems, customer relations, life sciences, product knowledge
• Experience: Minimum 2 years’ experience directly supporting interventional or surgical procedures within a hospital setting OR, 1 year of industry, hospital-based life sciences, sales support experience.
• Type: Fully Remote
• Salary: $100,000

Redwood City

• Skills: biological imaging, data acquisition, data pipelines, standardized imaging datasets, multi-PB image, data management, cross-functional project, big data, machine learning, image analysis
• Experience: 8+ years
• Type: Full-time
• Salary: 178,000 - 267,000

Menlo Park

• Skills: quantitative research, survey methodology, statistical inference, regression modeling, data analysis, research projects, cross-functional teams, measurement strategies, communicating insights, complex research questions
• Experience: 2+ years of post-graduation working experience
• Type: Full Time
• Salary: $145,000/year to $204,000/year + bonus + equity + benefits

San Francisco

• Skills: Data Management, Oncology, Data Integration, Collaboration, Compliance, Data Accuracy, Vendor Management, Project Management, Data Performance, Data Security
• Experience: Minimum of 6+ years of experience in data management, information systems, or commercial information management in the pharmaceutical industry.
• Type: Full time
• Salary: $120,800.00 to $201,400.00

Palo Alto

• Skills: Statistical Programming, CDISC SDTM, ADaM datasets, Clinical Trials, SAS programming, Data Analysis, Regulatory Submission, Clinical Study Reports, Data Integrity, Stakeholder Collaboration
• Experience: At least 10 years in pharmaceutical or bio-pharmaceutical industry with a bachelor’s degree in statistics, mathematics or equivalent, or at least 7 years with a master's degree.
• Salary: $170-180K/year

San Rafael

• Skills: clinical supply chain, drug forecasting, supply planning, team leadership, project management, regulatory compliance, vendor management, strategic vision, financial management, innovation
• Experience: Minimum of 7 years in Clinical Supply Chain / Contract Manufacturing operation in the pharmaceutical or biotech industry.
• Type: Hybrid
• Salary: $134,400 to $201,600

Santa Clara

• Skills: clinical research, project management, clinical trial, vendors, regulatory standards, protocol compliance, data collection, investigational sites, study design, clinical data
• Experience: Minimum 10 years’ experience directly supporting clinical research
• Type: Full-time

Newark

• Skills: clinical trials, study trackers, data verification, SOPs, clinical operations, protocol design, ICH/GCP regulations, teamwork, communication skills, Microsoft applications
• Experience: 2+ years in Clinical operations or healthcare-related experience
• Type: Full-time
• Salary: $85,000-$103,000

San Rafael

• Skills: medical writing, clinical studies, documentation, regulatory submissions, protocols, safety reports, cross-functional teams, drug development, clinical data, project management
• Experience: At least 5 years experience required
• Type: Full-time

San Francisco

• Skills: market research, competitive intelligence, biopharma, strategic insights, quantitative research, qualitative research, project management, patient focus, commercial planning, data analysis
• Experience: 5+ years of experience in the biopharma industry with relevant experience in primary market research (qual/quant) and competitive intelligence.
• Type: Full-time
• Salary: $170,000 - $215,000 USD

Millbrae

• Skills: clinical protocols, clinical study reports, investigator brochures, regulatory writing, document quality management, timelines, GCP guidelines, clinical development, project management, data interpretation
• Experience: 3+ years of relevant experience for Master's or 5+ years for Bachelor's degree.
• Type: Full-time
• Salary: $125,000 to $136,800

San Francisco

• Skills: market research, competitive intelligence, forecasting, analytics, business development, commercial strategy, data-driven decision-making, Hematology, Oncology, collaboration

San Rafael

• Skills: Clinical Development strategy, Program oversight, Project management, Team management, Recruitment strategies, Cross-functional collaboration, Drug Development, Clinical trials, Data analytics, Mentoring
• Experience: 10+ years clinical trial or drug development experience
• Type: Full-time
• Salary: $152,200 to $228,200

South San Francisco

• Skills: Medical Director, Rheumatology, Clinical Development, SLE program, TYK-2 inhibitor, Phase 2b study, Sponsor medical monitor, CRO collaboration, Data Monitoring Committee, Pharmacovigilance
• Experience: Licensed physician; Board certification in rheumatology or related field (desired); Industry experience in pharmacovigilance or clinical development (helpful).
• Salary: $285,000 - $325,000 USD annually

South San Francisco

• Skills: Toxicology, Bioanalytical, Nonclinical evaluations, Drug discovery, Pharma, Clinical trials, Regulatory, Leadership, Collaboration, Critical thinking
• Experience: 15+ years of post-training experience in academia, biotech or pharma.
• Type: Full-time
• Salary: $262,080 - $283,466 a year

San Francisco

• Skills: data management, Clinical Data Management, project planning, customer management, data quality, team leadership, financial management, global studies, service delivery, negotiation
• Experience: 7 years
• Type: Full time
• Salary: $82,300.00 - $173,900.00

San Francisco

• Skills: healthcare law, compliance, privacy, clinical trials, biopharmaceutical, FDA, Stark Law, Anti-Kickback Statute, pharmacovigilance, healthcare fraud
• Experience: 15+ years as healthcare law counsel at a biotechnology or pharmaceutical company and/or a law firm supporting pharmaceutical/biotech clients.
• Type: Full-time
• Salary: $235,500 - $329,500 per year

Redwood City

• Skills: Clinical Research, GCP, Regulatory Compliance, Data Verification, Site Monitoring, Clinical Trials, Recruitment Strategies, Document Maintenance, Audit Readiness, Collaboration
• Experience: Minimum of 4-6 years of experience in clinical research, including IVD experience.
• Type: Contract

Palo Alto

• Skills: Regulatory Affairs, BLA, NDA, clinical trials, strategic leadership, collaboration, pharmaceutical, biotechnology, lifecycle management, FDA
• Experience: Minimum 12 years of documented professional experience at a Regulatory Affairs leadership position within the pharmaceutical or biotechnology industry.

San Francisco

• Skills: clinical data management, CDM, clinical trials, data validation, FDA guidelines, ICH guidelines, SOPs, vendor management, eCRF design, pharmaceutical industry
• Experience: Minimum of 10 years of clinical data management experience within pharmaceutical industry
• Type: Full-time

San Francisco

• Skills: Data Management, Clinical Research, Biostatistics, Statistical Programming, Pharmaceutical, Clinical Trials, Project Leadership, Patient Care, Regulatory Compliance, Healthcare
• Type: Full-time

Palo Alto

• Skills: clinical data, measurement science, data engineering, analytics, clinical studies, diagnostic products, machine learning, software engineering, fragmentomics, health outcomes

Millbrae

• Skills: clinical data management, data collection, clinical trials, FDA/ICH guidelines, EDC systems, project management, metrics analysis, data quality, CDASH/CDISC, vendor management
• Experience: 6+ years with a Post Graduate degree or 8+ years with a Bachelor's degree in a relevant field
• Type: Full-time
• Salary: $152,000 to $166,250

San Francisco

• Skills: Clinical Pharmacology, quantitative pharmacology, drug development, PK/PD, clinical trials, multi-disciplinary collaboration, drug efficacy, safety data, regulatory guidance, biopharmaceutical
• Experience: 12+ years of industry or similar experience in Clinical Pharmacology or Quantitative Systems Pharmacology
• Type: Full-time

Palo Alto

• Skills: Real-World Data, evidence analytics, observational research, reimbursement, payer evidence, clinical development, key opinion leaders, statistical programs, data visualization, scientific publications

Hayward

• Skills: Safety, Pharmacovigilance, Medical Director, Risk management, Clinical trials, Oncology, Regulatory Authority, Signal detection, Cross-functional teams, Patient safety
• Experience: 3+ years’ relevant Safety experience required.
• Salary: $280,000 - $320,000

Menlo Park

• Skills: bioinformatics, next-generation sequencing, data analysis, molecular diagnostics, process automation, clinical data, Python, cloud computing, software development, data visualization
• Experience: PhD in Bioinformatics, Biostatistics, Computational Biology, Computer Science, Bioengineering, or other relevant field; 3-5 years of biology or bioinformatics research experience; 2-3 years of experience analyzing NGS data.
• Type: Full-time
• Salary: $244,805 per year

Palo Alto

• Skills: biostatistics, drug development, clinical study design, statistical analysis plans, exploratory analysis, FDA regulations, SAS programming, data analysis, cross-functional collaboration, clinical study reports
• Experience: PhD in statistics or equivalent, with at least 10 years of relevant experience in biotechnology or pharmaceutical industry
• Type: Full-time
• Salary: $225-240K/year

Menlo Park

• Skills: clinical data management, EDC system, data quality, study startup, data review, data queries, programming, regulatory requirements, data visualization, collaboration
• Experience: 5+ years
• Type: Full-time
• Salary: $105K - $131K for Menlo Park, CA

San Francisco

• Skills: healthcare, project management, implementation, SaaS, client management, clinical, data science, AI, medication management, health outcomes
• Experience: 3-5 years in healthcare management, delivery, and/or consulting; 3+ years of project management and/or implementation experience
• Type: Full-time
• Salary: $110,000-125,000/year

Hayward

• Skills: data analysis, health data standards, EMR, quality reports, data visualization, dashboards, HIPAA, healthcare, analytics, decision support
• Experience: Minimum of 3 years of experience in data analysis and decision support
• Type: Full-time
• Salary: $32.46 - $38.24 per hour